QC Stability Coordinator

Lonza Group Ltd.; Tampa (FL); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Career development

Cross-functional collaboration

Job summary

Lonza Group Ltd. in Tampa, FL is seeking a QC Stability Coordinator to manage stability studies, protocols, sample pulls, and storage conditions.

You will coordinate data review, trends, and inquiries, and collaborate with Quality Control, Quality Assurance, and Product Development to support study design and execution. Ideal candidates will have an associate degree or higher in a scientific discipline, GMP knowledge, strong analytical and communication skills, and experience in regulated

Qualifications

• Associate degree or higher in a scientific or related discipline.
• Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings.
• Knowledge of GMP and stability program requirements, including regulatory guidelines.
• Strong analytical skills with the ability to interpret data and identify trends.
• Ability to manage multiple priorities and coordinate activities across teams.
• Effective communication skills with both technical and non-technical stakeholders.
• Familiarity with data tools (e.g., Excel) and quality systems is preferred.

Responsibilities

• Coordinate and manage stability studies, including protocols, sample pulls, and storage conditions.
• Monitor stability data, identify trends, and elevate out-of-specification or out-of-trend results.
• Support audits by preparing documentation and responding to stability-related inquiries.
• Manage quality records such as deviations, CAPAs, and change controls within the stability program.
• Collaborate with Quality Control, Quality Assurance, and Product Development teams to support study design and execution.
• Maintain stability databases, dashboards, and performance metrics to ensure program visibility.
• Drive process improvements to enhance efficiency, compliance, and data reliability.

Skills

Analytical skills

Communication skills

GMP knowledge

Multi-tasking

Excel

Quality systems

Education

Associate degree or higher

in scientific discipline

Tools

Excel

Job description

QC Stability Coordinator

Location: Tampa, FL (on-site)

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

What you will get

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• Medical, dental and vision insurance.
• Opportunities to contribute to meaningful work that improves lives.
• Career development through cross-functional collaboration and continuous improvement initiatives.

The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits

What you will do

• You will coordinate and manage stability studies, including protocols, sample pulls, and storage conditions.
• You will monitor stability data, identify trends, and elevate out-of-specification or out-of-trend results.
• You will support audits by preparing documentation and responding to stability-related inquiries.
• You will manage quality records such as deviations, CAPAs, and change controls within the stability program.
• You will collaborate with Quality Control, Quality Assurance, and Product Development teams to support study design and execution.
• You will maintain stability databases, dashboards, and performance metrics to ensure program visibility.
• You will drive process improvements to enhance efficiency, compliance, and data reliability.

What we are looking for

• Associate degree or higher in a scientific or related discipline.
• Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings.
• Knowledge of GMP and stability program requirements, including regulatory guidelines.
• Strong analytical skills with the ability to interpret data and identify trends.
• Ability to manage multiple priorities and coordinate activities across teams.
• Effective communication skills with both technical and non-technical stakeholders.
• Familiarity with data tools (e.g., Excel) and quality systems is preferred.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. Every day, our teams across the world work together to turn scientific breakthroughs into life-changing medicines that reach up to 100 million patients a year. Lonza is a place where people can make a unique impact, grow their careers and belong. You will feel at home at Lonza if you:

• Take ownership, step forward, and enjoy meaningful responsibility
• Love solving problems and thrive in a complex, fast-moving environment
• Are curious, always looking to learn and improve
• Work collaboratively, contributing to something bigger than yourself
• Are motivated to make a difference through work that impacts customers and their patients

Why Lonza

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters. We are the makers of the medicines of tomorrow. Join us. Be you.